TY - JOUR
T1 - High temperature chromophore-embedded polyimides for use in second-order nonlinear optics
AU - Davey, M. H.
AU - Lee, V. Y.
AU - Wu, L. M.
AU - Moyla, C. R.
AU - Volksen, W.
AU - Knoesen, A.
AU - Miller, R. D.
AU - Marks, T. J.
N1 - Copyright:
Copyright 2004 Elsevier Science B.V., Amsterdam. All rights reserved.
PY - 2000/3
Y1 - 2000/3
N2 - Polyimides, especially functionalized aromatic polyimides are among the high temperature polymer systems attractive for high-Tg poled second-order nonlinear optical (NLO) materials. The incorporation of the three novel, chemically and thermally stable second-order NLO chromophore diamine monomers bis(4-aminophenyl)[4-(2-(4-nitrophenyl)vinyl)phenyl]amine, bis(4-aminophenyl)[4-(2-(6-nitrobenzothiazol-2-yl)vinyl)phenyl]amine, and 2-[4-((4-(bis(4-aminophenyl)amino)phenyl)diazenyl)phenyl]-2-phenyl -1,1-dicy anoethylene into the mainchain of six processable polyimides via a condensation reaction is described.
AB - Polyimides, especially functionalized aromatic polyimides are among the high temperature polymer systems attractive for high-Tg poled second-order nonlinear optical (NLO) materials. The incorporation of the three novel, chemically and thermally stable second-order NLO chromophore diamine monomers bis(4-aminophenyl)[4-(2-(4-nitrophenyl)vinyl)phenyl]amine, bis(4-aminophenyl)[4-(2-(6-nitrobenzothiazol-2-yl)vinyl)phenyl]amine, and 2-[4-((4-(bis(4-aminophenyl)amino)phenyl)diazenyl)phenyl]-2-phenyl -1,1-dicy anoethylene into the mainchain of six processable polyimides via a condensation reaction is described.
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M3 - Conference article
AN - SCOPUS:0033749960
SN - 0032-3934
VL - 41
SP - 853
EP - 854
JO - American Chemical Society, Polymer Preprints, Division of Polymer Chemistry
JF - American Chemical Society, Polymer Preprints, Division of Polymer Chemistry
IS - 1
T2 - The San Francisco Meeting
Y2 - 26 March 2000 through 31 March 2000
ER -